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rs879255396

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255396(A;C)
Make rs879255396(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position113902864
GeneAP4B1, DCLRE1B
is asnp
is mentioned by
dbSNPrs879255396
ebirs879255396
HLIrs879255396
Exacrs879255396
Varsomers879255396
Maprs879255396
PheGenIrs879255396
hapmaprs879255396
1000 genomesrs879255396
hgdprs879255396
ensemblrs879255396
gopubmedrs879255396
geneviewrs879255396
scholarrs879255396
googlers879255396
pharmgkbrs879255396
gwascentralrs879255396
openSNPrs879255396
23andMers879255396
23andMe allrs879255396
SNP Nexus

SNPshotrs879255396
SNPdbers879255396
MSV3drs879255396
GWAS Ctlgrs879255396
Max Magnitude0
ClinVar
Risk rs879255396(C;C)
Alt rs879255396(C;C)
Reference rs879255396(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DCLRE1B AP4B1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.114445486T>G
CLNSRC
CLNACC RCV000239291.1,